Takagi K, Nakao M, Ogura Y, Nabeshima T, Kunii A
Nagoya University College of Medical Technology, Japan.
Clin Chim Acta. 1994 Apr;226(1):67-75. doi: 10.1016/0009-8981(94)90103-1.
A simple and sensitive colorimetric assay for serum diamine oxidase (DAO) activity was based on a coupled reaction with peroxidase and a new chromogen, 10-(carboxymethyl-aminocarbonyl)-3,7-bis(dimethylamino) phenothiazine sodium salt (DA-67). In the presence of peroxidase and DA-67, peroxidase catalyzes the formation of methylene blue having an absorption maximum at 668 nm. The proposed method eliminates the interferences occurring in serum with use of ascorbate oxidase and stops the reaction with sodium diethyldithiocarbamate, leaving the methylene blue in the reaction mixture stable for about 2 h. Low normal basal values of serum DAO can be determined in the range 2.8-9.0 units/l. Since all reagents are commercially available the method is suitable for the clinical laboratory.
一种用于血清二胺氧化酶(DAO)活性的简单灵敏的比色测定法基于与过氧化物酶和一种新型显色剂10-(羧甲基-氨基羰基)-3,7-双(二甲基氨基)吩噻嗪钠盐(DA-67)的偶联反应。在过氧化物酶和DA-67存在下,过氧化物酶催化形成在668nm处有最大吸收的亚甲蓝。所提出的方法通过使用抗坏血酸氧化酶消除血清中发生的干扰,并使用二乙基二硫代氨基甲酸钠终止反应,使反应混合物中的亚甲蓝稳定约2小时。血清DAO的低正常基础值可在2.8-9.0单位/升范围内测定。由于所有试剂均可商购,该方法适用于临床实验室。